** = Publications listed in SCI/SSCI/Pubmed
** Jahic, A; Hinreiner, S; Emberger, W; Hehr, U; Zuchner, S; Beetz, C
Doublet-Mediated DNA Rearrangement-A Novel and Potentially Underestimated Mechanism for the Formation of Recurrent Pathogenic Deletions.
Hum Mutat. 2017; 38(3):275-278
Doi: 10.1002/humu.23162
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** Orendi, K; Emberger, W; Speicher, MR; Hoefler, G; Sill, H
Molecular Cytogenetics and Multiplex Reverse-Transcriptase Polymerase Chain Reaction for Risk Stratification in Acute Myeloid Leukemia.
J Clin Oncol. 2013; 31(18):2360-2361
Doi: 10.1200/JCO.2013.48.8189
[OPEN ACCESS]
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** Rankl, J; Flicker, K; Valentin, A; Horn, M; Uranus, S; Groselj-Strele, A; Emberger, W; Sill, H;
Hypersensitivity to alkylation treatment of primary fibroblasts from patients with therapy-related myeloid neoplasms.
Leuk Res. 2012; 36(7):e137-e139
Doi: 10.1016/j.leukres.2012.03.005
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** Reitter, S; Neumeister, P; Beham-Schmid, C; Emberger, W; Strunk, D; Brezinschek, R; Linkesch, W; Schmidt, HH
A case of generalized MALT lymphoma with IgM paraproteinemia and peripheral blood involvement.
Ann Hematol. 2010; 89(2): 213-214.
Doi: 10.1007/s00277-009-0787-6
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** Pichler, M; Beham-Schmid, C; Lackner, K; Linkesch, W; Fickert, P; Emberger, W; Schmidt, H
Cholestatic hepatitis due to diffuse liver infiltration by Acute myelogenous leukemia with inv(16)(p13;q22): A case report and review of the literature
ONKOLOGIE. 2010; 33: 141-141.-Jahrestagung der Deutschen, Österreichischen und Schweizerischen Gesellschaften für Hämatologie und Onkologie; Oct 1 -5, 2010; Berlin, Germany.
[Poster]
Web of Science
** Zinke-Cerwenka, W; Stojakovic, T; Rohn, A; Ziegler, I; Emberger, W; Sipurzynski, S; Linkesch, W; Neumeister, P
First-line treatment with bortezomib, doxorubicine and dexamethasone followed by autologous peripheral blood stem cell transplantation in newly diagnosed patients with multiple myeloma
BONE MARROW TRANSPLANT. 2010; 45(2):S149-S149.-36th Annual Meeting of the European Group for Blood and Marrow Transplantation; MAR 21-24, 2010; Vienna, AUSTRIA.
[Poster]
Web of Science
** Zacherl, M; Sourij, H; Beham, A; Emberger, W; Leithner, A; Windhager, W
Cerebrotendinous xanthomatosis. Hereditary lipid storage disease leading to bilateral swelling of Achilles tendon
Orthopade. 2008; 37(7):704-708
Doi: 10.1007/s00132-008-1275-8
(- Case Report)
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** Regauer, S; Emberger, W; Reich, O; Pfragner, R
Cytogenetic analyses of two new cases of endometrial stromal sarcoma--non-random reciprocal translocation t(10;17)(q22;p13) correlates with fibrous ESS.
Histopathology. 2008; 52(6):780-783
Doi: 10.1111/j.1365-2559.2008.03022.x
(- Case Report)
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** Deutsch, AJ; Aigelsreiter, A; Staber, PB; Beham, A; Linkesch, W; Guelly, C; Brezinschek, RI; Fruhwirth, M; Emberger, W; Buettner, M; Beham-Schmid, C; Neumeister, P
MALT lymphoma and extranodal diffuse large B-cell lymphoma are targeted by aberrant somatic hypermutation.
Blood. 2007; 109(8):3500-3504
Doi: 10.1182/blood-2006-06-030494
[OPEN ACCESS]
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** Schallmoser, K; Bartmann, C; Rohde, E; Reinisch, A; Kashofer, K; Emberger, W; Lanzer, G; Linkesch, W; Strunk, D
A novel system for highly efficient clinical scale propagation of human mesenchymal stem cells with human platelet lysate
HAEMATOL-HEMATOL J. 2007; 92: 317-318.-12th Congress of the European Hematology Association; JUN 7-10, 2007; Vienna, AUSTRIA.
[Poster]
Web of Science
** Schallmoser, K; Reinisch, A; Bartmann, C; Rohde, E; Kashofer, K; Emberger, W; Lanzer, G; Linkesch, W; Strunk, D
Animal serum-free clinical scale propagation of human MSC
TRANSFUSION. 2007; 47(3):28A-28A.-American Association of Blood Banks (AABB) 60th Annual Meeting; OKT 20-23, 2007; Anaheim, California, USA.
[Oral Communication]
Web of Science
** Zebisch, A; Staber, PB; Delavar, A; Bodner, C; Hiden, K; Fischereder, K; Janakiraman, M; Linkesch, W; Auner, HW; Emberger, W; Windpassinger, C; Schimek, MG; Hoefler, G; Troppmair, J; Sill, H
Two transforming C-RAF germ-line mutations identified in patients with therapy-related acute myeloid leukemia.
Cancer Res. 2006; 66(7):3401-3408
Doi: 10.1158/0008-5472.CAN-05-0115
[OPEN ACCESS]
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** Wölfler, A; Erkeland, SJ; Bodner, C; Valkhof, M; Renner, W; Leitner, C; Olipitz, W; Pfeilstöcker, M; Tinchon, C; Emberger, W; Linkesch, W; Touw, IP; Sill, H
A functional single-nucleotide polymorphism of the G-CSF receptor gene predisposes individuals to high-risk myelodysplastic syndrome.
Blood. 2005; 105(9):3731-3736
Doi: 10.1182/blood-2004-06-2094
[OPEN ACCESS]
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** Emberger, W; Regauer, S; Sodial, S; Reich, O; Zierler, H; Wagner, K; Pfragner, R
Endometrial stromal sarcoma: cytogenetic and molecular cytogenetic analyses
EUR J CELL BIOL 2005 84: 17-17.
Web of Science
** Zinke-Cerwenka, W; Neumeister, P; Eibl, M; Sill, H; Emberger, W; Wagner, T; Wolfler, A; Linkesch, W
Planned sequential autologous/non-myeloablative allogeneic peripheral stem cell transplantation in patients with newly diagnosed high-risk multiple myeloma
BONE MARROW TRANSPLANT 2005 35: S387-S388.
Web of Science
** Schmidt, HH; Strehl, S; Thaler, D; Strunk, D; Sill, H; Linkesch, W; Jäger, U; Sperr, W; Greinix, HT; König, M; Emberger, W; Haas, OA
RT-PCR and FISH analysis of acute myeloid leukemia with t(8;16)(p11;p13) and chimeric MOZ and CBP transcripts: breakpoint cluster region and clinical implications.
Leukemia. 2004; 18(6):1115-1121
Doi: 10.1038/sj.leu.2403353
(- Case Report)
[OPEN ACCESS]
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** Regauer, S; Emberger, W; Reich, O; Liegl, B; Pfragner, R
Cytogenetic characterization of mucosa-associated malignant melanomas
J INVEST DERMATOL 2004 122: A156-A156.
Web of Science
** Zebisch, A; Staber, PB; Fischereder, K; Bodner, C; Hiden, K; Linkesch, W; Auner, HW; Emberger, W; Windpassinger, C; Schimek, MG; Hoefler, G; Troppmair, J; Sill, H
Two novel activating germline mutations of the C-RAF proto-oncogene predisposing to solid tbmors and therapy-related acute myeloid leukemia.
BLOOD 2004 104: 920A-920A.
Doi: 10.1182/blood.V104.11.3370.3370
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** Emberger, W; Olipitz, W; Sodia, S; Petek, E; Zierler, H; Kroisel, PM; Wagner, K
Blast crisis in Philadelphia negative CML: Clinical findings and molecular cytogenetic characterization of a 47,XX,+i(11)(q10) cell line.
EUR J HUMAN GENET 2002 10: 105-106.
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** Sodia, S; Emberger, W; Rauter, L; Petek, E; Zierler, H; Wagner, K; Kroisel, PM
Constitutional mosaicism for a partial trisomy 8 in a patient with a Chromosome Breakage Syndrome
EUR J HUMAN GENET 2002 10: 130-130.
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** Emberger, W; Behmel, A; Tschernigg, M; Seewann, HL; Petek, E; Kroisel, PM; Wagner, K
Chronic myeloid leukemia with a rare variant Philadelphia translocation: t(9;10;22)(q34;q22;q11).
Cancer Genet Cytogenet. 2001; 129(1):76-79
Doi: 10.1016/S0165-4608(01)00417-4
(- Case Report)
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** Kroisel, PM; Petek, E; Emberger, W; Windpassinger, C; Wladika, W; Wagner, K
Candidate region for Gilles de la Tourette syndrome at 7q31.
Am J Med Genet. 2001; 101(3):259-261
Doi: 10.1002/1096-8628(20010701)101:3<259::AID-AJMG1374>3.0.CO;2-#
(- Case Report)
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** Emberger, W; Petek, E; Kroisel, PM; Zierler, H; Wagner, K
Clinical and molecular cytogenetic characterization of two patients with partial trisomy 1q41-qter: further delineation of partial trisomy 1q syndrome.
Am J Med Genet. 2001; 104(4):312-318
Doi: 10.1002/ajmg.10096
(- Case Report)
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** Emberger, W; Windpassinger, C; Petek, E; Kroisel, PM; Wagner, K
Assignment of the human GABAA receptor delta-subunit gene (GABRD) to chromosome band 1p36.3 distal to marker NIB1364 by radiation hybrid mapping.
Cytogenet Cell Genet. 2000; 89(3-4):281-282
Doi: 10.1159/000015636
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** Emberger, W; Petek, E; Plecko-Starting, B; Kroisel, PM; Zierler, H; Wagner, K
A de novo complex chromosomal rearrangement involving chromosomes 2, 3, and 10 associated with microcephaly and early onset spasticity.
J Med Genet. 2000; 37(11):892-896
Doi: 10.1136/jmg.37.11.892
(- Case Report)
[OPEN ACCESS]
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** Petek, E; Emberger, W; Kroisel, PM; Wagner, K
Assignment of STAC to human chromosome band 3p22.3 between D3S3718 and D3S1611.
Cytogenet Cell Genet. 1999; 84(3-4):184-185
Doi: 10.1159/000015252
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** Emberger, W; Petek, E; Kroisel, PM; Trojovsky, A; Zierler, H; Wagner, K
Phenotype correlation of two patients with partial trisomy 1(q41-qter) combined with partial monosomy 8(p23.3-pter) respectively partial monosomy 5(p13.3-pter)
CYTOGENET CELL GENET 1999 85: 147-147.
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** Trojovsky, A; Zierler, H; Häusler, M; Emberger, W; Kroisel, PM; Wagner, K
Chromosomal abnormalities found in prenatal diagnosis
CYTOGENET CELL GENET 1999 85: 60-60.
Web of Science